High Dephosphorylated-Uncarboxylated MGP in Hemodialysis patients: risk factors and response to vitamin K2, A pre-post intervention clinical trial

Abstract Background Vascular calcifications are highly prevalent in hemodialysis patients. Dephosphorylated-uncarboxylated MGP (dp-ucMGP) was found to increase in vitamin K-deficient patients and may be associated with vascular calcifications. Supplementation of hemodialysis patients with vitamin K2...

Full description

Bibliographic Details
Main Authors: Mabel Aoun, Maha Makki, Hiba Azar, Hiam Matta, Dania Nehme Chelala
Format: Article
Language:English
Published: BMC 2017-06-01
Series:BMC Nephrology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12882-017-0609-3
id doaj-9404980696be426ab25b48f10d473ed6
record_format Article
spelling doaj-9404980696be426ab25b48f10d473ed62020-11-24T23:26:36ZengBMCBMC Nephrology1471-23692017-06-0118111010.1186/s12882-017-0609-3High Dephosphorylated-Uncarboxylated MGP in Hemodialysis patients: risk factors and response to vitamin K2, A pre-post intervention clinical trialMabel Aoun0Maha Makki1Hiba Azar2Hiam Matta3Dania Nehme Chelala4Nephrology Department, Saint-Georges HospitalBiostatistics Unit, Clinical Research Institute, American University of Beirut Medical CenterNephrology Department, Hôtel Dieu de France, Beirut, Saint-Joseph UniversityLaboratory Division, Saint-Georges HospitalHead of the Nephrology Department, Hôtel Dieu de France, Beirut. Saint-Joseph UniversityAbstract Background Vascular calcifications are highly prevalent in hemodialysis patients. Dephosphorylated-uncarboxylated MGP (dp-ucMGP) was found to increase in vitamin K-deficient patients and may be associated with vascular calcifications. Supplementation of hemodialysis patients with vitamin K2 (menaquinone-7) has been studied in Europe with a maximum 61% drop of dp-ucMGP levels. The aim of this study is to assess first the drop of dp-ucMGP in an Eastern Mediterranean cohort after vitamin K2 treatment and second the correlation between baseline dp-ucMGP and vascular calcification score. Methods This is a prospective, pre-post intervention clinical trial involving 50 hemodialysis patients who received daily 360 μg of menaquinone-7 for 4 weeks. At baseline they were assessed for plasma dp-ucMGP levels and vascular calcification scores (AC-24) as well as for other demographic, clinical and biological variables. Dp-ucMGP levels were measured a second time at 4 weeks. Results At baseline, dp-ucMGP levels were extremely elevated with a median of 3179.15 (1825.25; 4339.50) pM and correlated significantly with AC-24 (Spearman’s rho = 0.43, P = 0.002). Using a bivariate regression analysis, the association between dp-ucMGP levels and AC-24 was most significant when comparing dp-ucMGP levels less than 1000 to those more than 1000 pM (P = 0.02). Dp-ucMGP levels higher than 5000 pM were significantly associated with females, patients with recent fracture and patients with lower serum albumin (respectively P = 0.02, 0.004 and 0.046). The average drop of dp-ucMGP at 4 weeks of treatment was found to be 86% with diabetics having the lowest drop rate (P = 0.01). Conclusion Vitamin K deficiency, as assessed by high dp-ucMGP levels, is profound in hemodialysis patients from the Eastern Mediterranean region and it is significantly correlated with vascular calcifications. Daily 360 μg of menaquinone-7, given for 4 weeks, effectively reduces dp-ucMGP in this population. Future studies are needed to assess the changes in vascular calcifications in hemodialysis patients treated with vitamin K2 over a longer follow-up period. Trial registration The clinical trial was registered on clinicaltrials.gov (Identification number NCT02876354 , on August 11, 2016).http://link.springer.com/article/10.1186/s12882-017-0609-3Dephosphorylated Uncarboxylated matrix Gla proteinPre-post intervention clinical trialHemodialysisMenaquinone-7Vascular calcificationsVitamin K2
collection DOAJ
language English
format Article
sources DOAJ
author Mabel Aoun
Maha Makki
Hiba Azar
Hiam Matta
Dania Nehme Chelala
spellingShingle Mabel Aoun
Maha Makki
Hiba Azar
Hiam Matta
Dania Nehme Chelala
High Dephosphorylated-Uncarboxylated MGP in Hemodialysis patients: risk factors and response to vitamin K2, A pre-post intervention clinical trial
BMC Nephrology
Dephosphorylated Uncarboxylated matrix Gla protein
Pre-post intervention clinical trial
Hemodialysis
Menaquinone-7
Vascular calcifications
Vitamin K2
author_facet Mabel Aoun
Maha Makki
Hiba Azar
Hiam Matta
Dania Nehme Chelala
author_sort Mabel Aoun
title High Dephosphorylated-Uncarboxylated MGP in Hemodialysis patients: risk factors and response to vitamin K2, A pre-post intervention clinical trial
title_short High Dephosphorylated-Uncarboxylated MGP in Hemodialysis patients: risk factors and response to vitamin K2, A pre-post intervention clinical trial
title_full High Dephosphorylated-Uncarboxylated MGP in Hemodialysis patients: risk factors and response to vitamin K2, A pre-post intervention clinical trial
title_fullStr High Dephosphorylated-Uncarboxylated MGP in Hemodialysis patients: risk factors and response to vitamin K2, A pre-post intervention clinical trial
title_full_unstemmed High Dephosphorylated-Uncarboxylated MGP in Hemodialysis patients: risk factors and response to vitamin K2, A pre-post intervention clinical trial
title_sort high dephosphorylated-uncarboxylated mgp in hemodialysis patients: risk factors and response to vitamin k2, a pre-post intervention clinical trial
publisher BMC
series BMC Nephrology
issn 1471-2369
publishDate 2017-06-01
description Abstract Background Vascular calcifications are highly prevalent in hemodialysis patients. Dephosphorylated-uncarboxylated MGP (dp-ucMGP) was found to increase in vitamin K-deficient patients and may be associated with vascular calcifications. Supplementation of hemodialysis patients with vitamin K2 (menaquinone-7) has been studied in Europe with a maximum 61% drop of dp-ucMGP levels. The aim of this study is to assess first the drop of dp-ucMGP in an Eastern Mediterranean cohort after vitamin K2 treatment and second the correlation between baseline dp-ucMGP and vascular calcification score. Methods This is a prospective, pre-post intervention clinical trial involving 50 hemodialysis patients who received daily 360 μg of menaquinone-7 for 4 weeks. At baseline they were assessed for plasma dp-ucMGP levels and vascular calcification scores (AC-24) as well as for other demographic, clinical and biological variables. Dp-ucMGP levels were measured a second time at 4 weeks. Results At baseline, dp-ucMGP levels were extremely elevated with a median of 3179.15 (1825.25; 4339.50) pM and correlated significantly with AC-24 (Spearman’s rho = 0.43, P = 0.002). Using a bivariate regression analysis, the association between dp-ucMGP levels and AC-24 was most significant when comparing dp-ucMGP levels less than 1000 to those more than 1000 pM (P = 0.02). Dp-ucMGP levels higher than 5000 pM were significantly associated with females, patients with recent fracture and patients with lower serum albumin (respectively P = 0.02, 0.004 and 0.046). The average drop of dp-ucMGP at 4 weeks of treatment was found to be 86% with diabetics having the lowest drop rate (P = 0.01). Conclusion Vitamin K deficiency, as assessed by high dp-ucMGP levels, is profound in hemodialysis patients from the Eastern Mediterranean region and it is significantly correlated with vascular calcifications. Daily 360 μg of menaquinone-7, given for 4 weeks, effectively reduces dp-ucMGP in this population. Future studies are needed to assess the changes in vascular calcifications in hemodialysis patients treated with vitamin K2 over a longer follow-up period. Trial registration The clinical trial was registered on clinicaltrials.gov (Identification number NCT02876354 , on August 11, 2016).
topic Dephosphorylated Uncarboxylated matrix Gla protein
Pre-post intervention clinical trial
Hemodialysis
Menaquinone-7
Vascular calcifications
Vitamin K2
url http://link.springer.com/article/10.1186/s12882-017-0609-3
work_keys_str_mv AT mabelaoun highdephosphorylateduncarboxylatedmgpinhemodialysispatientsriskfactorsandresponsetovitamink2aprepostinterventionclinicaltrial
AT mahamakki highdephosphorylateduncarboxylatedmgpinhemodialysispatientsriskfactorsandresponsetovitamink2aprepostinterventionclinicaltrial
AT hibaazar highdephosphorylateduncarboxylatedmgpinhemodialysispatientsriskfactorsandresponsetovitamink2aprepostinterventionclinicaltrial
AT hiammatta highdephosphorylateduncarboxylatedmgpinhemodialysispatientsriskfactorsandresponsetovitamink2aprepostinterventionclinicaltrial
AT danianehmechelala highdephosphorylateduncarboxylatedmgpinhemodialysispatientsriskfactorsandresponsetovitamink2aprepostinterventionclinicaltrial
_version_ 1725554332944826368